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CapSure™ CapSure™ Permanent Fixation System

CapSure™ Permanent Fixation System - 15 Permanent Fasteners

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1.844.8.BD.LIFE (1.844.823.5433)
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1.800.556.6756
BDISurgery@bd.com
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100 Crossings BoulevardWarwick, Rhode Island 02886United States
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1.844.8.BD.LIFE (1.844.823.5433)
Monday to Friday 8:15 AM to 6:00 PM EST
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1.800.531.4124
Custserv.davol@bd.com
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100 Crossings Boulevard, Warwick, Rhode Island 02886, United States
Overview
Permanent Fixation Redefined

CapSure™ provides surgeons the confidence they desire through strong and reliable fixation.

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Features and Benefits
Promotional Story
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References

1. Bench top data. Results many not correlate to performance in humans.

2 Preclinical data. Results may not correlate to performance in humans

Indications

The CapSure™ Permanent Fixation System is indicated for the approximation of soft tissue and fixation of surgical mesh to tissues during open or laparoscopic surgical procedures, such as hernia repair.

Contraindications

Carefully inspect the area in the vicinity of the tissue being fastened to avoid inadvertent penetration of underlying structures such as bone, nerves, vessels, and viscera. Use of the CapSure™ Permanent Fixation System in the close vicinity of such underlying structures is contraindicated. For reference, the length of the fastener below the fastener head is 3.2 mm, the fastener head is another 1 mm (total 4.2 mm).

Precautions

Adequate counter pressure should be applied on the target area. Avoid placing hand or finger directly over the area where fastener is being deployed to prevent injury. Use caution when applying the CapSure™ fastener over or in proximity to underlying bone, vessels, nerves, or viscera. The intended fixation site should be assessed to ensure that while the tissue is compressed the total distance from the surface of the tissue to any underlying structures is greater than the length of the CapSure™ fastener. Adverse Reactions

Adverse reactions and potential complications associated with fixation devices such as the CapSure™ Permanent Fixation System may include, but are not limited to the following: hemorrhage, pain, edema and erythema at wound site; septicemia/infection; hernia recurrence/wound dehiscence, erosion and allergic response in patients with known sensitivities to PEEK and metals contained in 316L stainless steel, including chromium, nickel, copper, and iron.

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Specification

GTIN - each

00801741094989

1

GTIN - Case

10801741094986

5


Quantity

5/cs


Dimensions

CapSure™ Permanent Fixation System - 15 Fasteners

GTIN

GTIN - each 00801741094989 1
GTIN - Case 10801741094986 5

Packaging

Quantity 5/cs

Product Basic Specification

Dimensions CapSure™ Permanent Fixation System - 15 Fasteners
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Related Products
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    OptiFix™ Absorbable Fixation System - 30 Absorbable Fasteners

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    OptiFix™ Absorbable Fixation System - 15 Absorbable Fasteners

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Product Complaints
North American Regional Complaint Center
1-844-8BD-LIFE (1-844-823-5433)
Things to Consider

If you are a patient or end user, you can contact us yourself, or you may have your caregiver or your physician do that for you. To help us process your
information quickly and effectively, please contact our customer complaints
team.

To better facilitate our investigation, please include the following information in your reporting:


  • Product Name and/or Catalog Number
  • Lot Number or Serial Number
  • Any injuries and/or Harm?
  • What is the issue you experienced?
  • Is the actual sample or sample representative available? (If possible, please send affected sample)
  • Contact name and phone number
Product Recalls
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